A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111465



Internal ID21294731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:127247455..127255061hg38UCSC Ensembl
Innerchr7:126887509..126895115hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg387607
hg197607
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086817
Samplessample360
Known GenesGRM8
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111465
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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